Variant report

Variant	nsv899164
Chromosome Location	chr12:63540476-63611633
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:436)
CpG islands
(count:794)
Chromatin interactive
region (count:10)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:436 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr12:63545234-63545470	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr12:63544074-63544342	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr12:63550104-63550132	GM12878	blood:	n/a	n/a
4	BRCA1	chr12:63600642-63601071	Hela-S3	cervix:	n/a	n/a
5	CBX3	chr12:63570065-63570332	K562	blood:	n/a	n/a
6	CEBPB	chr12:63554623-63554689	A549	lung:	n/a	n/a
7	CEBPB	chr12:63573010-63573086	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr12:63569647-63569844	HepG2	liver:	n/a	chr12:63569707-63569718
9	CEBPB	chr12:63600261-63601236	MCF-7	breast:	n/a	n/a
10	CEBPB	chr12:63600679-63601182	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr12:63600785-63601096	A549	lung:	n/a	n/a
12	CEBPB	chr12:63569649-63569765	A549	lung:	n/a	chr12:63569707-63569718
13	CEBPB	chr12:63607177-63607379	A549	lung:	n/a	n/a
14	CEBPB	chr12:63577350-63577566	HepG2	liver:	n/a	chr12:63577475-63577486
15	CEBPB	chr12:63572869-63573101	IMR90	lung:	n/a	n/a
16	CEBPB	chr12:63577407-63577618	A549	lung:	n/a	chr12:63577475-63577486
17	CEBPB	chr12:63600554-63601331	MCF-7	breast:	n/a	n/a
18	CEBPB	chr12:63572887-63573147	A549	lung:	n/a	n/a
19	CEBPB	chr12:63569654-63569734	IMR90	lung:	n/a	chr12:63569707-63569718
20	CEBPB	chr12:63572966-63573073	K562	blood:	n/a	n/a
21	CHD1	chr12:63544502-63544718	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr12:63543928-63544259	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr12:63544525-63544972	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr12:63600755-63601111	Hela-S3	cervix:	n/a	n/a
25	CTBP2	chr12:63543651-63545351	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr12:63545940-63546090	NB4	blood:	n/a	chr12:63546025-63546038
27	CTCF	chr12:63545940-63546090	RPTEC	kidney:	n/a	chr12:63546025-63546038
28	CTCF	chr12:63545940-63546090	Caco-2	colon:	n/a	chr12:63546025-63546038
29	CTCF	chr12:63545847-63546206	K562	blood:	n/a	chr12:63546025-63546038
30	CTCF	chr12:63545060-63545210	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr12:63545920-63546070	GM12874	blood:	n/a	chr12:63546025-63546038
32	CTCF	chr12:63545580-63545730	AG04450	lung:	n/a	n/a
33	CTCF	chr12:63545892-63546215	HUVEC	blood vessel:	n/a	chr12:63546025-63546038
34	CTCF	chr12:63545960-63546110	HMEC	breast:	n/a	chr12:63546025-63546038
35	CTCF	chr12:63545260-63545410	AG09319	gingival:	n/a	n/a
36	CTCF	chr12:63545872-63546147	GM19238	blood:	n/a	chr12:63546025-63546038
37	CTCF	chr12:63545960-63546110	HFF-Myc	foreskin:	n/a	chr12:63546025-63546038
38	CTCF	chr12:63545940-63546090	HA-sp	spinal cord:	n/a	chr12:63546025-63546038
39	CTCF	chr12:63545892-63546128	GM12892	blood:	n/a	chr12:63546025-63546038
40	CTCF	chr12:63545960-63546110	HCT-116	colon:	n/a	chr12:63546025-63546038
41	CTCF	chr12:63545960-63546110	HMF	breast:	n/a	chr12:63546025-63546038
42	CTCF	chr12:63545869-63546131	MCF-7	breast:	n/a	chr12:63546025-63546038
43	CTCF	chr12:63545826-63546202	A549	lung:	n/a	chr12:63546025-63546038
44	CTCF	chr12:63545888-63546141	HepG2	liver:	n/a	chr12:63546025-63546038
45	CTCF	chr12:63545696-63546400	SK-N-SH	brain:	n/a	chr12:63546025-63546038
46	CTCF	chr12:63545853-63546126	K562	blood:	n/a	chr12:63546025-63546038
47	CTCF	chr12:63545680-63545830	GM12874	blood:	n/a	n/a
48	CTCF	chr12:63545120-63545270	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr12:63546718-63546755	LNCaP	prostate:	n/a	n/a
50	CTCF	chr12:63545960-63546110	Hela-S3	cervix:	n/a	chr12:63546025-63546038

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:63545956-63546006	HRE	kidney:	n/a
2	chr12:63545956-63546006	HRE	kidney:	n/a
3	chr12:63544175-63544225	AG04449	skin:	fetal
4	chr12:63544319-63544369	RPTEC	kidney:	n/a
5	chr12:63544175-63544225	HepG2	liver:	n/a
6	chr12:63544319-63544369	AG09309	skin:	n/a
7	chr12:63545956-63546006	ECC-1	luminal epithelium:	n/a
8	chr12:63545288-63545338	HMEC	breast:	n/a
9	chr12:63546263-63546313	AG09319	gingival:	n/a
10	chr12:63546263-63546313	AoSMC	blood vessel:	n/a
11	chr12:63543831-63543881	HAEpiC	amniotic membrane:	n/a
12	chr12:63545288-63545338	K562	blood:	n/a
13	chr12:63544175-63544225	HUVEC	blood vessel:	n/a
14	chr12:63547716-63547766	LNCaP	prostate:	n/a
15	chr12:63545956-63546006	SK-N-MC	brain:	n/a
16	chr12:63543831-63543881	H1-hESC	embryonic stem cell:	embryo
17	chr12:63547716-63547766	AG04450	lung:	fetal
18	chr12:63545783-63545833	HUVEC	blood vessel:	n/a
19	chr12:63545288-63545338	NH-A	brain:	n/a
20	chr12:63544857-63544907	HIPEpiC	eye:	n/a
21	chr12:63544175-63544225	MCF-7	breast:	n/a
22	chr12:63544319-63544369	HPAEpiC	pulmonary alveolar:	n/a
23	chr12:63544319-63544369	SAEC	small airway:	n/a
24	chr12:63545288-63545338	T-47D	breast:	n/a
25	chr12:63544430-63544480	PANC-1	pancreas:	n/a
26	chr12:63544430-63544480	AG09309	skin:	n/a
27	chr12:63543831-63543881	A549	lung:	n/a
28	chr12:63545783-63545833	NT2-D1	testis:	n/a
29	chr12:63546263-63546313	RPTEC	kidney:	n/a
30	chr12:63545956-63546006	SKMC	muscle:	n/a
31	chr12:63544923-63544973	HNPCEpiC	eye:	n/a
32	chr12:63547716-63547766	NHBE	bronchial:	n/a
33	chr12:63544923-63544973	ovcar-3	ovarian:	n/a
34	chr12:63546263-63546313	GM12892	blood:	n/a
35	chr12:63547716-63547766	HAEpiC	amniotic membrane:	n/a
36	chr12:63545523-63545573	HNPCEpiC	eye:	n/a
37	chr12:63544175-63544225	NT2-D1	testis:	n/a
38	chr12:63543831-63543881	HEEpiC	esophagus:	n/a
39	chr12:63546263-63546313	GM12891	blood:	n/a
40	chr12:63545288-63545338	GM12878	blood:	n/a
41	chr12:63545783-63545833	MCF10A-Er-Src	breast:	n/a
42	chr12:63544857-63544907	CMK	blood:	n/a
43	chr12:63545783-63545833	GM19239	blood:	n/a
44	chr12:63545956-63546006	NB4	blood:	n/a
45	chr12:63544923-63544973	HepG2	liver:	n/a
46	chr12:63545783-63545833	Caco-2	colon:	n/a
47	chr12:63545523-63545573	HepG2	liver:	n/a
48	chr12:63543292-63543342	HepG2	liver:	n/a
49	chr12:63544319-63544369	HEEpiC	esophagus:	n/a
50	chr12:63544857-63544907	HUVEC	blood vessel:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:63545419..63546376-chr12:64195555..64196413,2	MCF-7	breast:
2	chr12:63545428..63546206-chr12:63674883..63675724,2	MCF-7	breast:
3	chr12:62996207..62999162-chr12:63547684..63549229,2	MCF-7	breast:
4	chr12:63599815..63602634-chr12:63602685..63604731,2	MCF-7	breast:
5	chr12:63535701..63537481-chr12:63551924..63553918,2	MCF-7	breast:
6	chr12:63540258..63542828-chr12:63547028..63548966,2	K562	blood:
7	chr12:63599815..63602634-chr12:63602685..63604731,2	MCF-7	breast:
8	chr12:63540258..63542828-chr12:63547028..63548966,2	K562	blood:
9	chr12:63545559..63546473-chr12:63669896..63671149,5	MCF-7	breast:
10	chr12:63545448..63546470-chr12:63670124..63671316,6	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM5-5	chr12:63563605-63563746	l_664_chr12:63563604-63657550_brain
2	lnc-MON2-3	chr12:63547640-63547786	ENSG00000257973.1
3	lnc-MON2-3	chr12:63546261-63546418	ENSG00000257973.1
4	lnc-MON2-3	chr12:63544845-63544872	ENSG00000257973.1
5	lnc-TMEM5-5	chr12:63580624-63580735	l_664_chr12:63563604-63657550_brain
6	lnc-TMEM5-5	chr12:63563762-63563912	l_664_chr12:63563604-63657550_brain

No data

Variant related genes	Relation type
AVPR1A	TF binding region
AVPR1A	CpG island
ENSG00000199179	chromatin interactions
ENSG00000221949	chromatin interactions
ENSG00000257354	chromatin interactions

Extended variants
information (count: 954 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:954 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11174811	chr12:63540476-63540477	Active TSS Genic enhancers Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs75197306	chr12:63540503-63540504	Active TSS Genic enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs528214854	chr12:63540515-63540516	Active TSS Genic enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs547981122	chr12:63540566-63540567	Active TSS Genic enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs373659196	chr12:63540579-63540580	Active TSS Genic enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs536931353	chr12:63540587-63540588	Active TSS Genic enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs557186765	chr12:63540624-63540625	Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs570678571	chr12:63540677-63540678	Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538977382	chr12:63540775-63540776	Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs78249943	chr12:63540803-63540804	Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559000770	chr12:63540830-63540831	Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs3803107	chr12:63540834-63540835	Weak transcription Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs541584059	chr12:63540847-63540848	Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs189748175	chr12:63540878-63540879	Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs113644739	chr12:63540910-63540911	Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146966736	chr12:63540914-63540915	Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs183114511	chr12:63540958-63540959	Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs137992996	chr12:63540960-63540961	Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs187299503	chr12:63540990-63540991	Weak transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs35856440	chr12:63541063-63541064	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527913816	chr12:63541080-63541081	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558973145	chr12:63541082-63541083	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373731451	chr12:63541123-63541124	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192411187	chr12:63541125-63541126	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs144329263	chr12:63541157-63541158	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs61734518	chr12:63541200-63541201	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs143654785	chr12:63541203-63541204	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs374551459	chr12:63541232-63541233	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs145917441	chr12:63541247-63541248	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs138652515	chr12:63541266-63541267	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs183401493	chr12:63541279-63541280	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs201493231	chr12:63541321-63541322	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs539390731	chr12:63541330-63541331	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs376412201	chr12:63541351-63541352	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs552601876	chr12:63541408-63541409	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs151327743	chr12:63541415-63541416	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs370281487	chr12:63541421-63541422	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs140679994	chr12:63541427-63541428	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs111347350	chr12:63541428-63541429	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs373666552	chr12:63541471-63541472	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs368118966	chr12:63541475-63541476	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs535103729	chr12:63541522-63541523	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs188849978	chr12:63541554-63541555	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs112962186	chr12:63541581-63541582	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs537603908	chr12:63541628-63541629	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs113732341	chr12:63541664-63541665	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs546023347	chr12:63541671-63541672	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs112546016	chr12:63541672-63541673	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs73136703	chr12:63541686-63541687	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs199980321	chr12:63541710-63541711	Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:422 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:63540200-63540600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr12:63540400-63540600	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
3	chr12:63540400-63541000	Genic enhancers	Liver	Liver
4	chr12:63540400-63541200	Active TSS	Psoas Muscle	Psoas
5	chr12:63540400-63543200	Active TSS	Adipose Nuclei	Adipose
6	chr12:63540600-63541000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr12:63541000-63541200	Weak transcription	Liver	Liver
8	chr12:63541000-63542600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr12:63541200-63541400	Flanking Active TSS	Liver	Liver
10	chr12:63541200-63541400	Flanking Active TSS	Psoas Muscle	Psoas
11	chr12:63541400-63543800	Active TSS	Liver	Liver
12	chr12:63541800-63542200	Weak transcription	Psoas Muscle	Psoas
13	chr12:63542000-63543200	Active TSS	Fetal Muscle Leg	muscle
14	chr12:63542200-63542400	Bivalent/Poised TSS	Fetal Brain Female	brain
15	chr12:63542200-63543400	Active TSS	Fetal Stomach	stomach
16	chr12:63542600-63543800	Bivalent/Poised TSS	Right Ventricle	heart
17	chr12:63542600-63545200	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr12:63542800-63545000	Bivalent Enhancer	Fetal Brain Male	brain
19	chr12:63543000-63543200	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
20	chr12:63543000-63543800	Bivalent/Poised TSS	Fetal Brain Female	brain
21	chr12:63543200-63543600	Active TSS	Fetal Muscle Trunk	muscle
22	chr12:63543200-63543600	Active TSS	Psoas Muscle	Psoas
23	chr12:63543200-63543800	Bivalent/Poised TSS	Adipose Nuclei	Adipose
24	chr12:63543200-63543800	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
25	chr12:63543200-63543800	Bivalent/Poised TSS	Left Ventricle	heart
26	chr12:63543200-63543800	Active TSS	Right Atrium	heart
27	chr12:63543200-63544000	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
28	chr12:63543200-63546400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
29	chr12:63543400-63543600	Enhancers	Pancreas	Pancrea
30	chr12:63543400-63543800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
31	chr12:63543400-63543800	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
32	chr12:63543400-63543800	Bivalent/Poised TSS	Fetal Stomach	stomach
33	chr12:63543400-63543800	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
34	chr12:63543600-63543800	Bivalent/Poised TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr12:63543600-63543800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr12:63543600-63543800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
37	chr12:63543600-63543800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
38	chr12:63543600-63543800	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
39	chr12:63543600-63543800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
40	chr12:63543600-63543800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr12:63543600-63543800	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
42	chr12:63543600-63543800	Bivalent Enhancer	Fetal Intestine Small	intestine
43	chr12:63543600-63543800	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
44	chr12:63543600-63543800	Enhancers	Gastric	stomach
45	chr12:63543600-63544000	Bivalent/Poised TSS	NHDF-Ad	bronchial
46	chr12:63543600-63544200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
47	chr12:63543600-63544200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
48	chr12:63543600-63544200	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
49	chr12:63543600-63544200	Bivalent Enhancer	Fetal Thymus	thymus
50	chr12:63543600-63544200	Bivalent/Poised TSS	Ovary	ovary

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